Our Leadership

Jeremy is the Vice President of Finance and brings 17 years of progressive experience leading teams and companies through complex transactions and SEC reporting compliance. Prior to Disc, Jeremy was a Partner at CFGI, the largest non-audit accounting advisory firm in the U.S. and a portfolio company of The Carlyle Group, providing accounting advisory and transaction services to public and private companies ranging from the Fortune 500 to seed-round startups, with a focus on life science companies. In this role, he was a national subject matter expert across a variety of complex accounting areas, led multinational public company implementations of the revenue and leasing standards, led and supported IPO readiness and acquisition integration, implemented financial systems and operationalized processes and controls across organizations. Prior to CFGI, Jeremy worked at Covidien, a $12 billion global health care device company, and began his career at PwC. He is a certified public accountant licensed in the Commonwealth of Massachusetts and received his B.S. in Accounting from the University of Utah.

Jason is the Head of Intellectual Property of Disc Medicine. Previously, Jason was Vice President of Intellectual Property at Acceleron Pharma, where he led intellectual property strategy development and worldwide implementation for the company’s commercial, clinical-stage, and pre-development programs. In particular, he led or supported a wide range of legal matters including patent strategy for Reblozyl®️ (luspatercept-aamt) and sotatercept (currently in development by Merck & Co. for treatment of pulmonary hypertension), building the company’s IP intellectual property team, and the successful acquisition of the company by Merck. Prior to Acceleron, Jason worked at the law firm of Ropes & Gray, where he helped clients in the biotechnology and pharmaceutical industries on a wide range of intellectual property issues, including patent portfolio development, life-cycle management, patent prosecution, patent listing and delisting matters, patent term restoration, patent litigation, and assessments regarding patentability, validity, non-infringement, and freedom-to-operate. He received a Ph.D. in Molecular Microbiology & Microbial Pathogenesis from Washington University in St. Louis.

Andeleeb is the Head of Global Regulatory Affairs and brings over 15 years of experience in Regulatory Affairs both in the pharmaceutical and biotechnology sectors. Prior to Disc, she had different roles in the regulatory departments of several companies such as Astellas, Sanofi/Genzyme and Novartis/Sandoz. She was responsible for multiple successful submissions to global health authorities, such as the FDA, EMA, PMDA, and many others. Her expertise extends across the entire product development lifecycle, encompassing early-stage development, late-stage development, and post-approval phases.

Andeleeb was responsible for developing regulatory strategies for drug development across a wide spectrum of therapeutic areas, encompassing both rare orphan diseases and more prevalent common diseases. She has also led the Innovative Medicines Initiative (IMI) project on optimizing R&D of advanced therapy medicinal products (ATMP) in collaboration with other pharma and biotech companies. Prior to her work in Regulatory Affairs, she contributed to drug discovery and R&D, utilizing her background as a pharmacist. Andeleeb holds a master’s degree in Drug Innovation from the University of Utrecht.

Rajiv is the Vice President of CMC and Clinical Supply Chain. He brings over a decade of experience in various aspects of CMC such as process, analytical, formulation and manufacturing across small/large molecules and cell therapies. Prior to Disc, Rajiv held roles of increasing responsibilities at Magenta Therapeutics where he served as the head of technical operations supporting GMP DS and DP manufacturing campaigns for a variety of therapeutic modalities (Peptides, Monoclonal Antibodies, ADCs, and Cell Therapies) in Ph1/2 clinical programs. Before Magenta, Rajiv was the head of Analytical CMC at Eleven Biotherapeutics (later Sesen Bio). At Eleven, Rajiv led CMC activities in support of Ph2/3 clinical programs involving monoclonal antibodies and Fusion proteins. Rajiv started his career at Akrivis Technologies where he led the development of Akrivis’s proprietary technology to target small size tumor lesions and cancer stem cells. His work at Akrivis resulted in multiple NIH/NCI awards.

Rajiv holds a BS in Pharmaceutical Sciences from MD University in India and MS/PhD in Interdisciplinary Pharmaceutical Sciences from Northeastern University in Boston.